Evidence map›Paper›PMID 31281317›Full record

ArticleFrontiers in immunology2019

Interleukin 33/ST2 Axis Components Are Associated to Desmoplasia, a Metastasis-Related Factor in Colorectal Cancer.

Glauben Landskron, Marjorie De la Fuente López, Karen Dubois-Camacho, David Díaz-Jiménez, Octavio Orellana-Serradell, Diego Romero, Santiago A Sepúlveda, Christian Salazar, Daniela Parada-Venegas, Rodrigo Quera and 11 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 35 citations in OpenAlex.

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  4. Advancements in 3D In Vitro Models for Colorectal Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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  5. Foods (Basel, Switzerland) · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 5 institutions in 2 countries.

Glauben LandskronImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Marjorie De la Fuente LópezImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Karen Dubois-CamachoImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
David Díaz-JiménezImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Octavio Orellana-SerradellImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Diego RomeroPathology Department, Faculty of Medicine, Pontificia Universidad Catolica de Chile, Santiago, Chile.
Santiago A SepúlvedaPathology Department, Faculty of Medicine, Pontificia Universidad Catolica de Chile, Santiago, Chile.
Christian SalazarImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Daniela Parada-VenegasImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
Rodrigo QueraInflammatory Bowel Disease Program, Gastroenterology Department, Clinica Las Condes, Santiago, Chile.
Daniela SimianResearch Sub-direction, Academic Direction, Clinica Las Condes, Santiago, Chile.
María-Julieta GonzálezCell and Molecular Biology Program, Faculty of Medicine, Institute of Biomedical Sciences, Universidad de Chile, Santiago, Chile.
Francisco López-KöstnerColoproctology Department, Clinica Las Condes, Santiago, Chile.
Udo KronbergColoproctology Department, Clinica Las Condes, Santiago, Chile.
Mario AbedrapoColoproctology Department, Clinica Las Condes, Santiago, Chile.
Iván GallegosPathology Department, Hospital Clinico Universidad de Chile, Santiago, Chile.
Héctor R ContrerasDepartment of Basic and Clinic Oncology, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Cristina PeñaMedical Oncology Department, Ramon y Cajal University Hospital, IRYCIS, CIBERONC, Madrid, Spain.
Guillermo Díaz-ArayaMolecular Pharmacology Laboratory, Faculty of Chemical Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.
Juan Carlos RoaPathology Department, Faculty of Medicine, Pontificia Universidad Catolica de Chile, Santiago, Chile.
Marcela A HermosoImmunology Program, Innate Immunity Laboratory, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile.
University of Chile · CLClínica Las Condes · CLPontificia Universidad Católica de Chile · CLCentro de Investigación Biomédica en Red de Cáncer · ESHospital Clínico de la Universidad de Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In colorectal cancer (CRC), cancer-associated fibroblasts (CAFs) are the most abundant component from the tumor microenvironment (TM). CAFs facilitate tumor progression by inducing angiogenesis, immune suppression and invasion, thus altering the organization/composition of the extracellular matrix (i.e., desmoplasia) and/or activating epithelial-mesenchymal transition (EMT). Soluble factors from the TM can also contribute to cell invasion through secretion of cytokines and recently, IL-33/ST2 pathway has gained huge interest as a protumor alarmin, promoting progression to metastasis by inducing changes in TM. Hence, we analyzed IL-33 and ST2 content in tumor and healthy tissue lysates and plasma from CRC patients. Tissue localization and distribution of these molecules was evaluated by immunohistochemistry (using localization reference markers α-smooth muscle actin or α-SMA and E-cadherin), and clinical/histopathological information was obtained from CRC patients.

Indexed as

AdultAgedCancer-Associated FibroblastsCell MovementCell ProliferationColorectal NeoplasmsFemaleHumansInterleukin-1 Receptor-Like 1 ProteinInterleukin-33MaleMiddle AgedNeoplasm InvasivenessTumor MicroenvironmentIL1RL1 protein, humanIL33 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33cancer associated fibroblastscolorectal cancerdesmoplasiaepithelial-mesenchymal transitioninterleukin 33

Identifiers

PMID31281317
PMCPMC6598075
OpenAlexW2948299089

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.